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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

SNCG Gene

protein-coding   GIFtS: 62
GCID: GC10P088708

synuclein, gamma (breast cancer-specific protein 1)

 Explore 44 diseases affiliated with
SNCG via our new
 Human Malady Compendium 
Biological research products
for SNCG
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
Synuclein, Gamma (Breast Cancer-Specific Protein 1)1 2     Synoretin3
BCSG11 2 3 5     PERSYN3
SR1 2 3     PRSN3
Persyn3     Persyn3
Breast Cancer-Specific Gene 1 Protein2 3     Synoretin3
Gamma-Synuclein1     

External Ids:    HGNC: 111411   Entrez Gene: 66232   Ensembl: ENSG000001732677   OMIM: 6029985   UniProtKB: O760703   

Export aliases for SNCG gene to outside databases

Previous GC identifers: GC10P087599 GC10P087941 GC10P088849 GC10P088382 GC10P082572


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for SNCG:
This gene encodes a member of the synuclein family of proteins which are believed to be involved in the pathogenesis of
neurodegenerative diseases. Mutations in this gene have also been associated with breast tumor development. (provided
by RefSeq, Jan 2010)

UniProtKB/Swiss-Prot: SYUG_HUMAN, O76070
Function: Plays a role in neurofilament network integrity. May be involved in modulating axonal architecture during
development and in the adult. In vitro, increases the susceptibility of neurofilament-H to calcium-dependent proteases
(By similarity). May also function in modulating the keratin network in skin. Activates the MAPK and Elk-1 signal
transduction pathway (By similarity)

Gene Wiki entry for SNCG (Gamma-synuclein)


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000010.10  NC_018921.1  NT_030059.13  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the SNCG gene promoter:
         HOXA9B   HOXA9   AML1a   C/EBPalpha   PPAR-gamma1   HSF2   Meis-1a   PPAR-gamma2   Meis-1   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidSNCG promoter sequence
   Search SABiosciences Chromatin IP Primers for SNCG

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat SNCG


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 10q23.2-q23.3   Ensembl cytogenetic band:  10q23.2   HGNC cytogenetic band: 10q23.2-q23.3

SNCG Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
SNCG gene location

GeneLoc information about chromosome 10         GeneLoc Exon Structure

GeneLoc location for GC10P088708:  view genomic region     (about GC identifiers)

Start:
88,718,288 bp from pter      End:
88,723,017 bp from pter
Size:
4,730 bases      Orientation:
plus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: SYUG_HUMAN, O76070 (See protein sequence)
Recommended Name: Gamma-synuclein  
Size: 127 amino acids; 13331 Da
Subunit: May be a centrosome-associated protein
Subcellular location: Cytoplasm, perinuclear region. Cytoplasm, cytoskeleton, centrosome. Cytoplasm, cytoskeleton,
spindle. Note=Associated with centrosomes in several interphase cells. In mitotic cells, localized to the poles of the
spindle
Secondary accessions: O15104 Q96P61

Explore the universe of human proteins at neXtProt for SNCG: NX_O76070

Post-translational modifications:

  • Phosphorylated. Phosphorylation by GRK5 appears to occur on residues distinct from the residue phosphorylated by other
  • kinases1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O76070

  • SNCG Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins: NP_003078.2  
    ENSEMBL proteins: 
     ENSP00000344658   ENSP00000361087  

    Human Recombinant Protein Products: 
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    OriGene Protein Over-expression Lysate: SNCG
    OriGene Custom Protein Services for SNCG 
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    Novus Biologicals SNCG Proteins
    Novus Biologicals SNCG Lysate
    Browse Sino Biological Recombinant Proteins
    ProSpec Recombinant Protein for SNCG
    Browse Proteins at Uscn

    Gene Ontology (GO): 5/8 cellular component terms (GO ID links to tree view) (see all 8):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0005737cytoplasm ----
    GO:0005815microtubule organizing center IEA--
    GO:0005819spindle IEA--
    GO:0005886plasma membrane IEA--
    GO:0030424axon ----


    SNCG for ontologies           About GeneDecksing



    SNCG Antibody Products: 
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    Browse ELISAs and CLIAs at Uscn


    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    SNCG for domains           About GeneDecksing

    2 InterPro domains/families:
     IPR002462 Synuclein_gamma
     IPR001058 Synuclein

    Graphical View of Domain Structure for InterPro Entry O76070

    ProtoNet protein and cluster: O76070

    1 Blocks protein family: IPB001058 Synuclein signature

    UniProtKB/Swiss-Prot: SYUG_HUMAN, O76070
    Similarity: Belongs to the synuclein family


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: SYUG_HUMAN, O76070
    Function: Plays a role in neurofilament network integrity. May be involved in modulating axonal architecture during
    development and in the adult. In vitro, increases the susceptibility of neurofilament-H to calcium-dependent proteases
    (By similarity). May also function in modulating the keratin network in skin. Activates the MAPK and Elk-1 signal
    transduction pathway (By similarity)

         Genatlas biochemistry entry for SNCG:
    gamma synuclein,expressed during pre and postnatal development in the cell bodies and axons of primary sensory
    neurons,sympathetic neurons and motoneurons of peripheral and central nervous system,predominantly expressed in
    substantia nigra,maybe involved in exocytosis of synaptic vesicles,putatively involved in the pathogenesis of
    neurodegenerative diseases (but not found in amyotrophic lateral sclerosis or familial Parkinson) and overexpressed in
    breast tumors

    miRNA
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    8/10 QIAGEN miScript miRNA Assays for microRNAs that regulate SNCG (see all 10):
    hsa-miR-3673 hsa-miR-15a hsa-miR-497 hsa-miR-103a hsa-miR-424 hsa-miR-15b* hsa-miR-195 hsa-miR-16
    SwitchGear 3'UTR luciferase reporter plasmidSNCG 3' UTR sequence
    Inhib. RNA
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    Search Advanced Cell Diagnostics for RNAscope RNA in situ hybridization assays for SNCG

    Gene Ontology (GO): 2 molecular function terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0043014alpha-tubulin binding IEA--
    GO:0048487beta-tubulin binding IEA--


    SNCG for ontologies           About GeneDecksing


    Animal Models:
         Mouse knock-out Sncgtm1Vlb for SNCG
         4 MGI mutant phenotypes (inferred from 1 allele(MGI details for Sncg):
     behavior/neurological  cellular  homeostasis/metabolism  nervous system 

    SNCG for phenotypes           About GeneDecksing


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section



    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for SNCG

    STRING Interaction Network Preview (showing 5 interactants - click image to see 22)

    5/25 Interacting proteins for SNCG (O760703 ENSP000003610874) via UniProtKB, MINT, STRING, and/or I2D (see all 25)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    MAPK1P284823, ENSP000002158324I2D: score=4 STRING: ENSP00000215832
    MAPK3P273613, ENSP000002630254I2D: score=4 STRING: ENSP00000263025
    MAPK8P459833, ENSP000003534834I2D: score=4 STRING: ENSP00000353483
    DYNLL1P631673, ENSP000002425774I2D: score=2 STRING: ENSP00000242577
    FUBP1Q96AE43, ENSP000003598044I2D: score=2 STRING: ENSP00000359804
    About this table

    Gene Ontology (GO): 5/9 biological process terms (GO ID links to tree view) (see all 9):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0002118aggressive behavior IEA--
    GO:0007268synaptic transmission IEA--
    GO:0008344adult locomotory behavior IEA--
    GO:0014059regulation of dopamine secretion IEA--
    GO:0042220response to cocaine IEA--


    SNCG for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section

    SNCG for compounds           About GeneDecksing

    Browse Small Molecules at EMD Millipore
    Browse drugs & compounds from Enzo Life Sciences

    Browse Tocris compounds for SNCG

    2 HMDB Compounds for SNCG    About this table
    CompoundSynonyms CAS #PubMed Ids
    CalciumCa (see all 2)7440-70-2--
    IronArmco iron (see all 19)7439-89-6--
    6 Novoseek chemical compound relationships for SNCG gene    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    5-aza-2'deoxycytidine 40.7 3 11526506 (1), 12566312 (1)
    paclitaxel 27.1 7 16773211 (3), 12121974 (2), 12959183 (1)
    estrogen 11.5 5 12873981 (3), 15231664 (1)
    agar 5.5 2 11016747 (1), 12970872 (1)
    iron 0 1 10934140 (1)
    tyrosine 0 2 12716427 (1), 16392036 (1)

    Search CenterWatch for drugs/clinical trials and news about SNCG / SYUG 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for SNCG gene: 
    NM_003087.2  

    Unigene Cluster for SNCG:

    Synuclein, gamma (breast cancer-specific protein 1)
    Hs.349470  [show with all ESTs]
    Unigene Representative Sequence: BU595229
    4 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000465679 ENST00000348795 ENST00000372017(uc001keb.2) ENST00000483064


    miRNA
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    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat SNCG
    8/10 QIAGEN miScript miRNA Assays for microRNAs that regulate SNCG (see all 10):
    hsa-miR-3673 hsa-miR-15a hsa-miR-497 hsa-miR-103a hsa-miR-424 hsa-miR-15b* hsa-miR-195 hsa-miR-16
    SwitchGear 3'UTR luciferase reporter plasmidSNCG 3' UTR sequence
    Inhib. RNA
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat SNCG
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat SNCG

    Additional cDNA sequence: 

    AF010126.1 AF017256.1 AF411524.1 AK223367.1 AK311652.1 AK312141.1 BC014098.2 CR541788.1 
    CR541790.1 EU019993.1 

    9 DOTS entries:

    DT.444070  DT.121238404  DT.95243972  DT.97843198  DT.121238422  DT.91744356  DT.95169337  DT.121238439 
    DT.99965408 

    24/267 AceView cDNA sequences (see all 267):

    AA486472 BE566379 BU728272 BM838642 AA878084 CR541788 BM748818 AI434794 
    CA434240 NM_006829 BQ219402 H49348 CR541790 BG413520 BQ430954 BQ694475 
    BQ218148 CB107161 CB045310 AI637713 BM693306 AB075855 AW006481 AJ346418 

    GeneLoc Exon Structure

    5/7 Alternative Splicing Database (ASD) splice patterns (SP) for SNCG (see all 7)    About this scheme

    ExUns: 1a · 1b · 1c · 1d ^ 2a · 2b · 2c ^ 3a · 3b · 3c · 3d ^ 4a · 4b ^ 5a · 5b · 5c · 5d
    SP1:                          -           -     -     -           -           -                           
    SP2:                          -           -     -                 -           -                           
    SP3:                          -           -                       -           -                           
    SP4:                          -           -     -     -           -                                       
    SP5:                                      -     -     -           -           -                           


    ECgene alternative splicing isoforms for SNCG

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    SNCG expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: CGGCTGCCCA

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image

    SNCG expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    10 LifeMap In Vivo Development Anatomical Compartments/Cells 
    Tissue Anatomical Compartment CellCategory (developmental path)
    EyeGanglion Cell LayerMature Ganglion CellsGanglion, Retina
    EyeInner Nuclear LayerMature Horizontal CellsHorizontal, Retina
    Spinal CordSpinal Ventral ColumnsVentral Spinal Cord Progenitor CellsMotor Neurons
    TestisSeminiferous TubulesSertoli cellsTestis
    AdiposeBody Subcutaneous White AdiposeAdipose
    AdiposeVisceral White AdiposeAdipose
    BrainMedulla OblongataBrain
    EyeRetinaEye
    Neural TubeMetencephalonNeural Tube
    Spinal CordSpinal Ventral ColumnsSpinal Cord
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 4 LifeMap Cells 
    NameCategory
    PureStem™ endothelial progenitor 30-MV2-12 (Embryonic Progenitor Cell)Blood, Endothelium
    PureStem™ endothelial progenitor 30-SM2-1 (Embryonic Progenitor Cell)Endothelium
    PureStem™ endothelial progenitor RP1-MV2-18 (Embryonic Progenitor Cell)Endothelium
    Ventral/hypothalamic-like neurons (Generation of midbra...)

    See SNCG Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for SNCG

    SOURCE GeneReport for Unigene cluster: Hs.349470

    UniProtKB/Swiss-Prot: SYUG_HUMAN, O76070
    Tissue specificity: Highly expressed in brain, particularly in the substantia nigra. Also expressed in the corpus
    callosum, heart, skeletal muscle, ovary, testis, colon and spleen. Weak expression in pancreas, kidney and lung

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    In Situ
    Assay Products:
     

     
    Search Advanced Cell Diagnostics for RNAscope RNA in situ hybridization assays for SNCG

    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of chordates.

    Orthologs for SNCG gene from 3/10 species (see all 10)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves SNCG1 synuclein, gamma (breast cancer-specific protein 1) 75.89(n)
    82.14(a)
      395392  NM_204672.1  NP_990003.1 
    lizard
    (Anolis carolinensis)
    Reptilia SNCG6
    --
    82(a)
    1 ↔ 1
    GL343199.1(4208583-4233082)
    zebrafish
    (Danio rerio)
    Actinopterygii BG306962.12   -- 74.25(n)    BG306962.1 


    ENSEMBL Gene Tree for SNCG (if available)
    TreeFam Gene Tree for SNCG (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for SNCG gene
    SNCB2  SNCA2  
    3 SIMAP similar genes for SNCG using alignment to 4 protein entries:     SYUG_HUMAN (see all proteins):
    NACP    SNCA    SNCB

    SNCG for paralogs           About GeneDecksing



    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/139 NCBI SNPs in SNCG are shown (see all 139    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 10 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs733536321,2
    C,--82571282(+) GGGGCC/TGCCAA 1 -- us2k11Minor allele frequency- T:0.50WA 2
    rs741504161,2
    C,--82571764(+) CCCTAC/TCTAGG 1 -- us2k12Minor allele frequency- T:0.08WA 120
    rs1138054681,2
    C,--82572156(+) CGCTGC/TGGCAG 1 -- us2k10--------
    rs797424561,2
    F,--82572595(+) GACAGG/AGCTGG 1 -- us2k13Minor allele frequency- A:0.13CSA WA 123
    rs788017161,2
    F,--82572714(+) CACACG/AGGAGC 1 -- us2k11Minor allele frequency- A:0.07WA 118
    rs1127400071,2
    F,--82572977(+) CCCCAC/AATTCT 1 -- us2k12Minor allele frequency- A:0.50CSA 4
    rs1114040921,2
    --82573073(+) CCTTAT/CCCCCC 1 -- us2k11Minor allele frequency- C:0.00CSA 1
    rs733349311,2
    C,--82576455(+) TCAGGG/ATGGCC 1 -- int12Minor allele frequency- A:0.03WA 120
    rs102321,2
    C,--82576654(+) NNNNTC/TCCTGG 1 -- ut31 ese33Minor allele frequency- T:0.04MN NA 306
    rs748892761,2
    --82576851(+) CCCAGG/TTCCTC 1 -- ds50010--------

    HapMap Linkage Disequilibrium report for SNCG (88718288 - 88723017 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 5 variations for SNCG
         5 CNVs: 6891 48665 48663 3815 48664

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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    SNCG for disorders           About GeneDecksing

    OMIM gene information: 602998    OMIM disorders: --

    20/44 diseases for SNCG (see all 44):    About MalaCards
    neurodegenerative disease    breast cancer    dendritic cell sarcoma    follicular dendritic cell sarcoma
    lewy body dementia    multiple system atrophy    corpus callosum    amyotrophic lateral sclerosis
    lateral sclerosis    esophageal squamous cell carcinoma    squamous cell carcinoma    pancreatic ductal adenocarcinoma
    glaucoma    amyloidosis    gaucher's disease    neurodegeneration
    parkinson's disease    dementia    ovarian endometriosis    ovarian carcinoma

    3 diseases from the University of Copenhagen DISEASES database for SNCG:
    Parkinson's disease     Lewy body dementia     Multiple system atrophy

    10/30 Novoseek disease relationships for SNCG gene (see all 30)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    neurodegenerative diseases 73 17 11091093 (1), 11369507 (1), 17681534 (1), 12559990 (1) (see all 14)
    parkinson disease 71.9 14 10557341 (2), 17681534 (1), 19711118 (1), 10852916 (1) (see all 13)
    multiple system atrophy 70.7 1 9749615 (1)
    lewy body disease 66.9 4 18577885 (2), 10557341 (1)
    breast carcinoma 57.7 28 12072430 (2), 11526506 (2), 16773211 (2), 17234772 (1) (see all 14)
    neurodegeneration 53.3 4 19246516 (1), 10934140 (1), 9700196 (1)
    alzheimers disease 52.7 11 11433431 (2), 9044857 (1), 10777786 (1), 18461469 (1) (see all 9)
    dementia 49.8 4 18577885 (2), 17681539 (1), 10557341 (1)
    breast cancer 46.8 97 14504205 (6), 16142440 (6), 16821081 (5), 17534899 (5) (see all 22)
    fibrillation 42.5 5 17088319 (3), 11812782 (1)

    Genetic Association Database (GAD): SNCG
    Human Genome Epidemiology (HuGE) Navigator: SNCG (6 documents)
    Tumor Gene Database (TGDB): SNCG

    Export disorders for SNCG gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for SNCG gene, integrated from 9 sources (see all 146):
    (articles sorted by number of sources associating them with SNCG)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Organization, expression and polymorphism of the human persyn gene. (PubMed id 9700196)1, 2, 3, 9 Ninkina N.N.... Buchman V.L. (1998)
    2. Identification of a breast cancer-specific gene, BCSG1, by direct differential cDNA sequencing. (PubMed id 9044857)1, 2, 3, 9 Ji H.... Shi Y.E. (1997)
    3. Gamma synuclein: subcellular localization in neuronal and non- neuronal cells and effect on signal transduction. (PubMed id 11746666)1, 2, 9 Surguchov A.... Surgucheva I. (2001)
    4. Identification, localization and characterization of the human gamma- synuclein gene. (PubMed id 9737786)1, 2, 9 Lavedan C.... Polymeropoulos M.H. (1998)
    5. Synucleins are a novel class of substrates for G protein-coupled receptor kinases. (PubMed id 10852916)1, 2, 9 Pronin A.N.... Benovic J.L. (2000)
    6. The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)1, 2 Gerhard D.S....Malek J. (2004)
    7. [Study on gamma-synuclein gene in patients with idiopathic Parkinson's disease] (PubMed id 14556204)1, 4 Su J.J....Ren D.M. (2003)
    8. Evaluation of the gamma-synuclein gene in German Parkinson's disease patients. (PubMed id 11585599)1, 4 Kruger R....Riess O. (2001)
    9. Expression of neuronal protein synuclein gamma gene as a novel marker for breast cancer prognosis. (PubMed id 16821081)1, 9 Wu K....Shi Y.E. (2007)
    10. Blockade of AP1 transactivation abrogates the abnormal expression of breast cancer-specific gene 1 in breast cancer cells. (PubMed id 12072430)1, 9 Lu A....Liu J. (2002)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 6623 HGNC: 11141 AceView: SNCGandC10orf116andKIAA1975 Ensembl:ENSG00000173267 euGenes: HUgn6623
    ECgene: SNCG H-InvDB: SNCG

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for SNCG Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for SNCG Genetics and Cytogenetics in Oncology and Haematology

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for SNCG gene:
    Search GeneIP for patents involving SNCG

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



    (Antibodies, recombinant proteins, and assays from EMD Millipore, R&D Systems, OriGene, QIAGEN, GenScript, Cell Signaling Technology, SABiosciences, Novus Biologicals, Sino Biological, Enzo Life Sciences, Abcam, ProSpec, Uscn, Thermo Fisher Scientific, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, GenScript, Sino Biological, DNA2.0, SwitchGear Genomics, Vector BioLabs, Cell lines from GenScript and LifeMap BioReagents, PCR Arrays from SABiosciences, Drugs and/or compounds from EMD Millipore, Tocris Bioscience, and/or Enzo Life Sciences),
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    About This Section

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